laerdal 801-00233 Скачать руководство пользователя страница 17

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Regulatory Information

Regulatory Information

      Cautions  
• 

Do not apply the CPRmeter 2 to an open wound or recent incision site.

• 

The device is designed to be used only with Laerdal-approved accessories 

and may perform improperly if non-approved accessories are used. Do 

not attempt to modify the device in any way.

• 

Use only model 801-10850 Patient Adhesives with the CPRmeter 2. 

 

Note

Changes or modifications not expressly approved by Laerdal Medical could 

void the user’s authority to operate the equipment.

 

Recommendation

Responders should receive training, including regular refresher training, 

in use of the CPRmeter 2.  When training with the device on a CPR 

manikin, disable or ignore feedback from the manikin.  

 

      WEEE

This appliance is marked according to the European directive 2012/19/EU on 

Waste Electrical and Electronic Equipment (WEEE).

By ensuring this product is disposed of correctly, you will help prevent 

potential negative consequences for the environment and human health, 

which could otherwise be caused by inappropriate waste handling of this 

product.

The symbol on the product indicates that this appliance may not be treated 

as household waste. Instead it shall be handed over to the applicable 

collection point for the recycling of electrical and electronic equipment.

Disposal must be carried out in accordance with local environmental 

regulations for waste disposal.

For more detailed information about treatment, recovery and recycling of this 

product, please contact your local city office, your household waste disposal 

service or the Laerdal representative where you purchased the product.

FCC

 

Federal Communications Commission Statement and Industry 
Canada Statements

This device complies with part 15 of the FCC rules and RSS-210 of the 
Industry Canada rules. Operation is subject to the following two conditions: 

1.  This device may not cause harmful interference, and
2.  this device must accept any interference received, including interference 

that may cause undesired operation.

Ce dispositif est conforme à la norme CNR-210 d’Industrie Canada 
applicable aux appareils radio exempts de licence. Son fonctionnement est 
sujet aux deux conditions suivantes: 

1.  Le dispositif ne doit pas produire de brouillage préjudiciable, et
2.  ce dispositif doit accepter tout brouillage reçu, y compris un brouillage 

susceptible de provoquer un fonctionnement indésirable.

This equipment has been tested and found to comply with the limits for 
a Class B digital device, pursuant to part 15 of the FCC Rules. These limits 
are designed to provide reasonable protection against harmful interference 
in a residential installation. This equipment generates, uses and can radiate 
radio frequency energy and, if not installed and used in accordance with 
the instructions, may cause harmful interference to radio communications. 
However, there is no guarantee that interference will not occur in a 
particular installation. If this equipment does cause harmful interference 
to radio or television reception, which can be determined by turning 
the equipment off and on, the user is encouraged to try to correct the 
interference by one or more of the following measures:

•  Reorient or relocate the receiving antenna.
•  Increase the separation between the equipment and receiver.
•  Consult the dealer or an experienced radio/TV technician for help.

FCC ID: QHQ-801002
IC ID: 20263-801002
The term ”IC” before the equipment certification number only signifies that 
the Industry Canada technical specifications were met.

Содержание 801-00233

Страница 1: ...CPRmeter 2 User Guide EN www laerdal com...

Страница 2: ...d 12 CPRmeter 2 Placement 13 Feedback Display Overview 15 Compression Feedback 16 Depth 16 On Soft Surface 17 Rate 18 Compression Counter 18 Inactivity 19 Debriefing 20 Battery Indicator 22 Maintenanc...

Страница 3: ...number of compressions in a series and provides notification of lack of expected CPR activity If in doubt about the appropriateness for use perform CPR without using the CPRmeter 2 Indication for Use...

Страница 4: ...6 7 Items Included Items Included A A A X 2 Protective Sleeve Patient Adhesive AAA Batteries CPRmeter 2...

Страница 5: ...8 9 Overview Overview On Off Status Light Compression Area Battery Hatch Display Area Placement guide for adhesive Placement guide for adhesive Membrane Port...

Страница 6: ...se Insert Batteries Before Use Apply Patient Adhesive 1 1 x 2 2 4 3 1 3 2 Cautions Ensure Patient Adhesives are within their expiration date Adhesives should be removed from the device and disposed of...

Страница 7: ...rface Remove clothing from the patient s chest Turn On Place CPRmeter 2 If needed wipe fluids off the chest Ensure to use the heel of your hand and apply pressure to the light grey area Begin CPR Prov...

Страница 8: ...pport after the event Warnings Do not use the device in conjunction with any mechanical or automated compression device Do not use the device on top of defibrillation pads unless the manufacturer of t...

Страница 9: ...ensuring that for each chest compression the area below the compression depth target lights up Warning When performing CPR on a patient lying on a mattress a backboard must be used to limit the amoun...

Страница 10: ...r digits flash solid white for every tenth compression Without a compression the counter is reset after 3 seconds Inactivity After 3 seconds the CPRmeter 2 displays an inactivity timer which counts th...

Страница 11: ...Rmeter 2 is turned off When turned on again the statistics from the last stored CPR event can be reviewed When the CPRmeter 2 is used in a new CPR event the Q CPR Quick Review will display the current...

Страница 12: ...en the CPRmeter 2 is being turned on 23 Note If the remaining battery power during use becomes too low to sustain further operation the low battery icon is shown for 10 seconds and then the CPRmeter 2...

Страница 13: ...erior surfaces and allow to sit for a minimum of 12 minutes An alternative disinfection agent is isopropyl alcohol 70 solution If necessary respray to account for evaporation of isopropyl alcohol 2 Wi...

Страница 14: ...C to 40 C 32 F to 104 F Sealing Meets ISO IEC 60529 class IP55 Product temperature can reach 60 C 140 F Relative Humidity Transport 5 to 95 Storage 5 to 75 Operation 5 to 95 Atmospheric Pressure Atm...

Страница 15: ...Directive 1999 5 EC Compliance with applicable U S and Canadian safety standards has been certified by Canadian Standards Association These CPRmeter 2 patient adhesives are disposable and are for sin...

Страница 16: ...t necessary to remove the device from the patient Do not practice by using the CPRmeter 2 on a person It may be used with a training manikin or simply on a compliant surface for practice Properly perf...

Страница 17: ...ion Statement and Industry Canada Statements This device complies with part 15 of the FCC rules and RSS 210 of the Industry Canada rules Operation is subject to the following two conditions 1 This dev...

Страница 18: ...dings used for domestic purposes Electromagnetic Immunity Immunity Test IEC 60601 Test Level Compliance Level Electromagnetic Environment Guidance Electrostatic Discharge ESD IEC 61000 4 2 6 kV contac...

Страница 19: ...nt Electromagnetic Emissions Rated maximum output power of transmitter W Separation distance according to frequency of transmitter m 150 kHz to 80 MHz 80 MHz to 800 MHz d 1 2 P 800 MHz to 2 5 GHz d 2...

Страница 20: ...s applies to the model 801 00233 CPRmeter 2 This information is subject to change The CPRmeter with Q CPR is protected by U S and International registered patents The design of CPRmeter and its feedba...

Страница 21: ...Rev A Laerdal is a registered trademark of Laerdal Medical AS 2015 Laerdal Medical AS All rights reserved P O Box 377 Tanke Svilandsgate 30 4002 Stavanger Norway T 47 51511700 Printed in Norway www la...

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